Amine-boranes bearing borane-intolerant functionalities

ABSTRACT

Disclosed herein is the preparation of functional group containing amine-boranes from the corresponding amines. The mild reaction conditions allow for the direct preparation of several hitherto inaccessible amine-boranes containing a functional moiety, such as but not limited to, alkene, alkyne, hydroxyl, thiol, acetal, ester, amide, nitrile, nitro, and alkoxysilane.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present U.S. patent application is a divisional of U.S.Non-Provisional Patent Application Ser. No. 15/680,259, filed Aug. 18,2017, which is related to and claims the priority benefit of U.S.Provisional Patent Application Ser. No. 62/377,290, filed Aug. 19, 2016,the contents of which are hereby incorporated by reference in theirentirety into the present disclosure.

TECHNICAL FIELD

The present invention relates to a process for the preparation of anamine-borane, specifically, an amine-borane bearing a functionality,such as alkene, alkyne, hydroxyl, thiol, acetal, ester, amide, nitrile,nitro, or alkoxysilane, under mild conditions. Products of this facileprocess are also in the scope of this disclosure.

BACKGROUND

This section introduces aspects that may help facilitate a betterunderstanding of the disclosure. Accordingly, these statements are to beread in this light and are not to be understood as admissions about whatis or is not prior art.

Amine-boranes have gained considerable importance as potentialcandidates for hydrogen storage. Moreover, they have been evaluated asreagents in organic chemistry and materials chemistry. (Carboni andMonnier, Tetrahedron, 1999, 55, 1197; Staubitz, et al., Chem. Rev. 2010,110, 4023) Amine-boranes have also shown promise as safe energeticmaterials. (Ramachandran et al., Chem. Eur. J. 2014, 20, 16869)

Current approaches to amine-boranes from amines include exchange withborane-Lewis base complexes or metathesis of alkylammonium salts withmetal borohydrides. The former necessitates the use ofmoisture-sensitive and pyrophoric borane-tetrahydrofuran (BTHF) orborane-dimethyl sulfide (BMS), or harsh reaction conditions with thestable borane-ammonia complex (AB). The poor solubility of sodiumborohydride and alkylammonium salts in common organic solvents severelyrestricts the generality of the metathesis protocol. To circumventthese, we recently discovered and disclosed a scalable protocol toaccess amine-boranes via an in situ generation of carbonic acid fromsodium bicarbonate and water (Ramachandran et al., U.S. Patentapplication 2016/0101984, dated Apr. 14, 2016).

Despite these advances in their synthesis and application, boranecomplexes of amines bearing functional groups are rare. This alsorestricts the use of borane as an amine-protecting group for organicchemistry applications. Thus, a convenient approach to functionalizedamine-boranes would be highly appreciated by the scientific community.

SUMMARY OF INVENTION

The present invention relates to a process for the preparation of anamine-borane complex, specifically, an amine-borane bearing afunctionality, such as alkene, alkyne, hydroxyl, thiol, acetal, ester,amide, nitrile, nitro, alkoxysilane, etc., under mild conditions.Products of this facile process are also in the scope of thisdisclosure.

In some aspects, this invention relates to a process for the preparationof an amine-borane bearing a functionality by the steps of

-   -   a. adding about two equivalent of sodium borohydride and four        equivalents of sodium bicarbonate;    -   b. adding about one equivalent amine, wherein said amine may        carry a functional group selected from the group consisting of        alkene, alkyne, nitro, hydroxyl, thiol, cyano (nitrile), acetal,        ester, amide, and alkoxysilane;    -   c. adding THF (tetrahydrofuran) with stirring to afford a        reaction mixture of said amine at about 0.5˜2 M (moles/liter);    -   d. adding about 3˜4 equivalents of water in a THF solution        dropwise to the reaction mixture of step c under vigorous        stirring; and    -   e. stirring for about 4 to 48 hours to afford an amine-borane,        wherein said amine-borane carries a functional group selected        from the group consisting of alkene, alkyne, nitro, hydroxyl,        thiol, cyano (nitrile), acetal, ester, amide, and alkoxysilane.

In some aspects, this invention relates to a process for the preparationof an amine-borane bearing a functionality by the process disclosedherein, wherein said amine-borane carries one or more functional groupsselected from the group consisting of alkene, alkyne, nitro, hydroxyl,thiol, cyano (nitrile), acetal, ester, amide, and alkoxysilane.

In some other aspects, this invention relates to a functionality-bearingamine-borane synthesized by the following process:

-   -   a. adding about two equivalent of sodium borohydride and four        equivalents of sodium bicarbonate;    -   b. adding about one equivalent amine, wherein said amine may        carry a functional group selected from the group consisting of,        but not limited to alkene, alkyne, nitro, hydroxyl, thiol, cyano        (nitrile), acetal, ester, amide, and alkoxysilane;    -   c. adding THF (tetrahydrofuran) with stirring to afford a        reaction mixture of said amine at about 0.5˜2 M (moles/liter);    -   d. adding about 3˜4 equivalents of water in a THF solution        dropwise to the reaction mixture of step c under vigorous        stirring; and    -   e. stirring for about 4 to 48 hours to afford an amine-borane,        wherein said amine-borane carries a functional group selected        from the group consisting of alkene, alkyne, nitro, hydroxyl,        thiol, cyano (nitrile), acetal, ester, amide, and alkoxysilane.

In some aspects, this invention relates to an amine-borane bearing oneor more functional groups selected from the group consisting of alkene,alkyne, nitro, hydroxyl, thiol, cyano (nitrile), acetal, ester, amide,and alkoxysilane.

DETAILED DESCRIPTION

For the purposes of promoting an understanding of the principles of thepresent disclosure, reference will now be made to the embodimentsillustrated in the drawings, and specific language will be used todescribe the same. It will nevertheless be understood that no limitationof the scope of this disclosure is thereby intended.

In the present disclosure, the term “about” can allow for a degree ofvariability in a value or range, for example, within 10%, within 5%, orwithin 1% of a stated value or of a stated limit of a range.

In the present disclosure, the term “substantially” can allow for adegree of variability in a value or range, for example, within 80%,within 90%, within 95%, or within 99% of a stated value or of a statedlimit of a range.

Disclosed herein is the preparation of functional group containingamine-boranes from the corresponding amines. The mild reactionconditions allow direct preparation of several hitherto inaccessibleamine-boranes containing a functional moiety such as, but not limited toalkene, alkyne, hydroxyl, thiol, acetal, ester, amide, nitrile, nitro,and alkoxysilane.

In some illustrative embodiments, this present invention relates to aprocess for preparing an amine-borane, comprising the steps of

-   -   a. adding about two equivalent of sodium borohydride and about        four equivalents of sodium bicarbonate;    -   b. adding about one equivalent amine, wherein said amine may        carry a functional group selected from the group consisting of,        but not limited to alkene, alkyne, nitro, hydroxyl, thiol, cyano        (nitrile), acetal, ester, amide, and alkoxysilane;    -   c. adding THF (tetrahydrofuran) with stirring to afford a        reaction mixture of said amine at about 0.5˜2 M (moles/liter);    -   d. adding dropwise about 3˜4 equivalents of water in a THF        solution to the reaction mixture of step c under vigorous        stirring; and    -   e. stirring for about 4 to 48 hours to afford an amine-borane,        wherein said amine-borane carries a functional group selected        from the group consisting of, but not limited to alkene, alkyne,        nitro, hydroxyl, thiol, cyano (nitrile), acetal, ester, amide,        and alkoxysilane.

In some illustrative embodiments, this present invention relates to aprocess for preparing an amine-borane disclosed herein, whereinwater-THF solution is about 14% (v/v) water in THF.

In some illustrative embodiments, this present invention relates to aprocess for preparing an amine-borane disclosed herein, wherein saidamine is a monoamine or a diamine.

In some illustrative embodiments, this present invention relates to aprocess for preparing an amine-borane disclosed herein, wherein saidprocess is performed at an ambient temperature.

In some illustrative embodiments, this present invention relates to aprocess for preparing an amine-borane disclosed herein, wherein saidamine-borane is part of an aromatic molecule, an aliphatic molecule, ora combination thereof.

In some illustrative embodiments, this present invention relates to aprocess for preparing an amine-borane disclosed herein, wherein saidamine-borane is part of a cyclic structure, a linear structure, abranched structure, or a combination thereof.

In some illustrative embodiments, this present invention relates to aprocess for preparing an amine-borane disclosed herein, wherein saidwater in a THF solution is about four equivalents of said amine whensaid amine carries a functional group selected from the group consistingof, but not limited to alkene, alkyne, nitro, hydroxyl, thiol, cyano(nitrile), acetal, ester, amide, and alkoxysilane.

In some aspects, this invention relates to a process for the preparationof an amine-borane bearing one or more functional groups selected fromthe group consisting of alkene, alkyne, nitro, hydroxyl, thiol, cyano(nitrile), acetal, ester, amide, and alkoxysilane.

In some illustrative embodiments, this present invention relates to anamine-borane prepared according to the process of

-   -   a. preparing about two equivalent of sodium borohydride and        about four equivalents of sodium bicarbonate;    -   b. adding about one equivalent amine, wherein said amine may        carry a functional group selected from the group consisting of,        but not limited to alkene, alkyne, nitro, hydroxyl, thiol, cyano        (nitrile), acetal, ester, amide, and alkoxysilane;    -   c. adding THF (tetrahydrofuran) with stirring to afford a        reaction mixture of said amine at about 0.5˜2 M (moles/liter);    -   d. adding dropwise about 3˜4 equivalents of water in a THF        solution to the reaction mixture of step c under vigorous        stirring; and    -   e. stirring for about 4 to 48 hours to afford an amine-borane,        wherein said amine-borane may carry a functional group selected        from the group consisting of, but not limited to alkene, alkyne,        nitro, hydroxyl, thiol, cyano (nitrile), acetal, ester, amide,        and alkoxysilane.

In some illustrative embodiments, this present invention relates to anamine-borane prepared according to the process disclosed herein, whereinsaid process is carried out at an ambient temperature.

In some illustrative embodiments, this present invention relates to anamine-borane prepared according to the process disclosed herein, whereinthe water-THF solution is about 14% (v/v) water in THF.

In some illustrative embodiments, this present invention relates to anamine-borane prepared according to the process disclosed herein, whereinsaid amine may be a monoamine or a diamine.

In some illustrative embodiments, this present invention relates to anamine-borane prepared according to the process disclosed herein, whereinsaid amine-borane is part of an aromatic molecule, an aliphaticmolecule, or a combination thereof.

In some illustrative embodiments, this present invention relates to anamine-borane prepared according to the process disclosed herein, whereinsaid amine-borane is part of a cyclic structure, a linear structure, abranched structure, or a combination thereof.

In some illustrative embodiments, this present invention relates to anamine-borane prepared according to the process disclosed herein, whereinsaid water in a THF solution is about four equivalents of said aminewhen said amine carries a functional group selected from the groupconsisting of, but not limited to alkene, alkyne, nitro, hydroxyl,thiol, cyano (nitrile), acetal, ester, amide, and alkoxysilane.

In some aspects, this invention relates to an amine-borane bearing oneor more functional groups selected from the group consisting of alkene,alkyne, nitro, hydroxyl, thiol, cyano (nitrile), acetal, ester, amide,and alkoxysilane.

The following examples and specific embodiments are intended toillustrate the above invention and should not be construed as to narrowits scope. One skilled in the art will readily recognize that theExamples suggest many other ways in which the invention could bepracticed.

It should be understood that numerous variations and modifications maybe made while remaining within the scope of the invention.

We recently realized an amine-ammonium salt equilibration-metathesissequence to access amine-boranes under open-flask conditions (Scheme 1,Ramachandran, et al., Inorg. Chem. 2015, 54, 5618). Although formationof the alkylammonium sulfate intermediate occurred at ambientconditions, elevated temperatures were necessary to trans-aminate thebyproduct AB formed via a competing pathway.

We envisaged that mild acids, such as carbonic acid, prepared fromsodium bicarbonate and water (K. Adamczyk, M. Premont-Schwarz, D. Pines,E. Pines and E. T. J. Nibbering, Science, 2009, 326, 1690), in thepresence of an amine could provide alkylammonium bicarbonate in situ.This would then undergo metathesis with NaBH₄ at room temperature toprovide the corresponding amine-borane (Scheme 2). Key to the success ofour plan would be the capture of carbonic acid by amine prior to itsready decomposition and the stability of NaBH₄ under mildly acidicreaction conditions. The increased probability of a facile saltmetathesis due to the solubilization of NaBH₄ and alkylammoniumbicarbonate in wet solvent looked promising. Treating an equiv. each ofNaBH₄ and N,N,N-triethylamine (la) with two equiv. of NaHCO₃ in 1 MTHF-H₂O (1:1 v/v) for 1 h revealed, by ¹¹B NMR spectroscopy, completeconsumption of NaBH₄ and the presence of ca. 3:1 mixture ofN,N,N-triethylamine-borane (Et₃N-BH₃, ¹¹B: δ −14 ppm, 2a) and twoimpurities, probably hydrolysis byproducts (δ 8 and δ 18 ppm). When thequantity of water was limited to one equiv., the impurities werecompletely suppressed and pure 2a was isolated in 77% yield. Loweringthe equiv. of NaHCO3 led to longer reaction times and lower yields. Theorder of addition was critical. Adding amine to a mixture of NaBH₄,NaHCO₃, and water in THF resulted in the borohydride hydrolysisproducts. Na₂CO₃ was found ineffective for this transformation. Effortsto improve the yield of 2a by screening several mono and dibasic sodiumand potassium salts of mineral acids proved futile. Replacing NaBH₄ withKBH₄ also led to slow reactions and poor yields. Increasing the reactionconcentration to 2 or 4 M or using diethyl ether as the solvent did notafford appreciable alteration.

Finally, a reaction with 2 equiv. of NaHCO₃ in 2 M THF was chosen forfurther improvement. On the basis of our envisioned pathway (Scheme 2),water should play a critical role in promoting the reaction. Indeed, areaction without water, even after 2 d, yielded only traces of 2a.Introducing 0.5 equiv. water completed the reaction, albeit slowly,within 24 h. Conversely, increasing the water content to 2 equiv.accelerated the reaction dramatically, complete within 1 h, to yield 82%2a. Further increase in water content was detrimental to the yield. Lessthan quantitative yields of 2a remained a concern. To investigate thesame, the filter cake was dissolved in water and analyzed by ¹¹ B NMRspectroscopy, which revealed the presence of a borate salt (δ 8 ppm).This was attributed to the hydrolysis of a portion of NaBH₄ under themildly acidic conditions. To ensure complete conversion to amine-borane,the effect of excess NaBH₄ was studied. 4-(Dimethylamino) pyridine(DMAP, 1b), a high-boiling amine, was chosen to prevent loss of residualamine during workup. At least 1.5 equiv. of NaBH₄ was necessary forquantitative conversion to DMAP-borane complex (2b). Significantly, evenwith excess NaBH₄, no borane complexation was observed at the lessnucleophilic nitrogen in DMAP.

The putative lack of formation of free borane persuaded us to subjectamines containing borane-susceptible functionalities to the newsynthesis, after a minor reoptimization of the reagent equivalencies(Table 1). Alkenyl and alkynyl amines, with an exposed hydroborationsite, were examined first.9 Gratifyingly, allylamine (1q),1,2,3,6-tetrahydropyridine (1r), and propargylamine (1s) yielded thecorresponding amine-boranes 2q, 2r, and 2s in 96%, 73%, and 87%,respectively, within 4 h. Delightfully, even amines containing theprotic hydroxyl moiety, such as, 2-(hydroxymethyl)pyridine (1t),3-aminopropan-1-ol (1u), and (S)-(+)-2-(hydroxymethyl)pyrrolidine (1v),underwent borane protection yielding 2t, 2u, and 2v, respectively, ingood yields after chromatographic purification.11 This represents thefirst general route to hydroxyl-containing amine-boranes from thecorresponding amino alcohols.

Extending the protocol to the more acidic thiol moiety in2-diethylaminoethanethiol (1w) provided the borane adduct 2w in highyields with a minor amount of the disulfide linked amine-borane, whichcould be readily separated by column chromatography. Amines containingthe aldehyde and ketone functionalities were, unfortunately, notcompatible and provided the reduced borane protected aminoalcohols.Dimethylaminoacetaldehyde acetal (1x), a protected aldehyde, whensubjected to the reaction conditions, yielded 96% of 2x. Pleasantly, thecarbonyl moiety in the ester and amide functionalities in methyl6-aminohexanoate (1y) and N-(3-aminopropyl)benzamide (1z) waswell-tolerated, furnishing 2y and 2z in 84% and 86% yields,respectively. The nitrile group in 3-(dimethylamino)propanenitrile (1aa)also remained unaltered under the reaction conditions providing thecorresponding amine-borane 2aa in 86% yield. Neither the nitrile-boranenor nitrile reduction products were observed.

Finally, we subjected 2-(4-nitrophenyl)ethylamine (1ab), an aminecontaining a nitro group, to our protocol, which underwent facile boraneprotection to yield 2ab in 86% yield. Notably, the amineboranessynthesized above represent stable molecules containing potentiallyincompatible electrophilic and nucleophilic centers in proximity.

The uniqueness of our robust and mild protocol was demonstrated by thefacile synthesis of the vitronectin inhibitor synthon 4 (Scheme 3). Thepresence of the protic hydroxyl group was an impediment to its readysynthesis earlier. Our NaHCO₃/water-mediated protocol described hereinprovides a direct route to 4 in 80% yield from pyridinylamino alcohol 3via the selective protection of the pyridine ring. The ready access tofunctionalized amine-boranes offered a new class of unexplored, reactivereagents for surface functionalization.

TABLE 1 Scope of Functionalized Amines^(a)

^(a)Yields of isolated product. ^(b)1.5 equiv. NaBH₄, 3 equiv. NaHCO₃,and 3 equiv. water were used for 1 equiv. of amine. ^(c)Diastereomericratio = 92:8 (by ¹¹B NMR spectroscopy). ^(d)20% disulfide containingamine-borane was formed.

In conclusion, a general, convenient, inexpensive, and scalable protocolfor the synthesis of a variety of amine-boranes in excellent yields fromsodium borohydride, sodium bicarbonate, and amines in wet THF has beendeveloped. Under these environmentally benign, mild reaction conditions,several functional groups susceptible to BTHF or BMS, such as alkene,alkyne, hydroxyl, thiol, ester, amide, nitrile, and nitro are welltolerated. Some of these functionalized amine-boranes represent stablemolecules bearing potentially incompatible electrophilic andnucleophilic groups in proximity. This water-promoted synthesis hasallowed access to a novel class of amine-borane based organic ligandswith unique properties for surface functionalization, as demonstrated bythe formation of self-assembled layers of thiol- andalkoxysilane-bearing amine-boranes on gold and silica surfaces,respectively.

General Experimental Procedures

¹¹B, ¹H, and ¹³C NMR spectra were recorded at room temperature, on aVarian INOVA 300 MHz or Bruker 400 MHz NMR spectrophotometer. Chemicalshifts (δ values) are reported in parts per million relative to BF₃.Et₂Ofor ¹¹B NMR respectively. Data are reported as: δ value, multiplicity(s=singlet, d=doublet, t=triplet, q=quartet, p=pentet, h=hextet,m=multiplet, br=broad) and integration. High Resolution Mass Spectra(HRMS) were recorded on a Thermo Electron Corporation MAT 95XP-Trapspectrometer. Thin-layer chromatography was carried out on 0.20 mmsilica plates (G/UV254) using UV light or Iodine as visualizing agent.Flash chromatography was performed using silica gel 40-63 um, 60 Å anddichloromethane-methanol mixture as eluent.

All solvents for routine isolation of products and chromatography werereagent-grade. Tetrahydrofuran (THF, ACS grade containing 0.004% waterand 0.025% BHT) was purchased from Fisher-Scientific. Sodium borohydride(powder, purity >99% by hydride estimationl) was purchased in bulk fromDow Chemical Co. (Rohm and Haas). Sodium bicarbonate (ACS reagent,Macron), sodium carbonate (Anhydrous, Macron), sodium bisulfite(Purified, Mallinckrodt), sodium hydrogen sulfate (tech. grade,Sigma-Aldrich), potassium bicarbonate (ACS, Sigma-Aldrich), dipotassiumhydrogen phosphate (Anhydrous, Fluka), and potassium dihydrogenphosphate (Assay >99.5%, Fluka) were purchased from the respectivecommercial sources and powdered prior to use. Amines used were purchasedfrom commercial sources. Methyl 6-aminohexanoate (1y) (Brehm andBreinbauer, Org. Biomol. Chem., 2013, 11, 4750.);N-(3-aminopropyl)benzamide (1z) (Tang and Fang, Tetrahedron Lett., 2008,49, 6003); 3-(pyridin-2-ylamino)propanol (3) (Heckmann, et al., Angew.Chem. Int. Ed., 2007, 46, 3571) was prepared in accordance withliterature reports. 2-Diethylaminoethanethiol (1w) (Bigley, et al.,Biochemistry, 2015, 54, 5502); and 2-(4-nitrophenyl)ethylamine (1ab)(Maruyama, et al., U.S. Pat. No. 6,346,532 (2002)) were synthesized fromtheir hydrochloride salts. Liquid amines were distilled while solidamines were used without any purification.

General procedure for the preparation of functionalized amine-boranes(2a, 2p, 2r-2w, 2y-2z, 2ab-2ac, and 4):

Sodium borohydride (0.38 g, 10 mmol) and powdered sodium bicarbonate(1.68 g, 20 mmol) were transferred to a 50 mL dry round bottom flask,charged with a magnetic stir-bar. The corresponding amine (1a, 1p,1r-1w, 1y-1z, 1ab-1ac, and 3, 5 mmol) was charged into the reactionflask followed by addition of reagent-grade tetrahydrofuran (2.5 mL forliquid amines/7.5 mL for solid amines) at rt. Under vigorous stirring,2.5 mL of 14.4% v/v solution water in THF was added drop-wise to preventexcessive frothing. Reaction progress was monitored by ¹¹B NMRspectroscopy (Note: A drop of anhydrous DMSO is added to the reactionaliquot before running the ¹¹B NMR experiment). Upon completion of thereaction (4-48 h, as determined by ¹¹B NMR), the reaction contents werefiltered through sodium sulfate and celite and the solid residue washedwith THF. Removal of the solvent in vacuo from the filtrate yielded thecorresponding crude amine-borane. Amine-boranes 2a and 2p did not needany further purification. The rest were purified by columnchromatography using dichloromethane/methanol mixture as eluent.

Characterization of amine-boranes:

Allylamine-borane (2q) Colorless oil. ¹H NMR (300 MHz, CDCl₃) δ (ppm):5.95 (ddt, J=16.7, 10.3, 6.3 Hz, 1H), 5.39-5.18 (m, 2H), 4.29-3.95 (m,2H), 3.46-3.27 (m, 2H), 2.10-0.90 (br q, BH₃); ¹³C NMR (75 MHz, CDCl₃) δ(ppm): 132.3, 119.3, 51.0; ¹¹B NMR (96 MHz, CDCl₃) δ (ppm): −19.81 (q,J=97.7 Hz). HRMS (CI) calcd for C₃H₉BN (M−H)⁺: m/z, 70.0823, found70.0826.

1,2,3,6-tetrahydropyridine-borane (2r) White solid. ¹H NMR (400 MHz,DMSO-d₆) δ (ppm): 6.10 (s, 1H), 5.84-5.70 (m, 1H), 5.69-5.53 (m, 1H),3.35-3.14 (m, 1H), 3.11-2.79 (m, 2H), 2.52-2.36 (m, 1H), 2.30-2.16 (m,1H), 2.10-1.90 (m, 1H), 1.80-0.80 (br q, BH₃); ¹³C NMR (101 MHz,DMSO-d₆) δ (ppm): 124.9, 123.6, 50.1, 48.3, 23.3; ¹¹B NMR (96 MHz,DMSO-d₆) δ (ppm): −14.48 (br q, J=95.0 Hz). HRMS (CI) calcd for C₅H₁₁BN(M−H)⁺: m/z, 96.0979, found 96.0976.

Propargylamine-borane (2s) White solid. ¹H NMR (300 MHz, DMSO-d₆) δ(ppm): δ 5.71 (s, 2H), 3.50-2.97 (m, 3H), 1.90-0.50 (br q, BH₃); ¹³C NMR(75 MHz, DMSO-d₆) δ (ppm): 79.6, 75.5, 36.2; ¹¹B NMR (96 MHz, DMSO-d₆) δ(ppm): −18.69 (br q). HRMS (CI) calcd for C₃H₇BN (M−H)⁺: m/z, 68.0666,found 68.0669.

2-(Hydroxymethyl)pyridine-borane (2t) White solid. ¹H NMR (300 MHz,CDCl₃) δ (ppm): 8.65 (d, J=5.8 Hz, 1H), 8.02-7.91 (m, 1H), 7.85-7.75 (m,1H), 7.44-7.32 (m, 1H), 5.03 (s, 2H), 3.17 (s, 1H), 3.00-1.75 (br q,BH₃); ¹³C NMR (75 MHz, CDCl₃) δ (ppm): 158.6, 148.8, 140.0, 123.5,123.4, 62.5; ¹¹B NMR (96 MHz, CDCl₃) δ (ppm): −15.23 (q, J=98 Hz). HRMS(CI) calcd for C₆H₉BNO (M−H)⁺: m/z, 122.0772, found 122.0772.

3-Aminopropan-1-ol-borane (2u) Colorless oil. ¹H NMR (400 MHz, DMSO-d₆)δ (ppm): 5.09 (s, 2H), 4.49 (t, J=5.0 Hz, 1H), 3.40 (q, J=5.9 Hz, 2H),2.58-2.35 (m, 2H), 1.61 (p; J=6.5 Hz, 2H), 1.70-0.80 (br q, BH₃); ¹³CNMR (101 MHz, DMSO-d₆) δ (ppm): 59.6, 46.3, 32.1; ¹¹B NMR (96 MHz,DMSO-d₆) δ (ppm): −19.59 (q, J=93.5 Hz). HRMS (CI) calcd for C₃H₁₁BNO(M−H)⁺: m/z, 88.0928, found 88.0926.

(S)-(+)-2-(Hydroxymethyl)pyrrolidine-borane (2v) Colorless oil.Diastereomeric ratio =92:8 (as analyzed by ¹¹B NMR spectroscopy). Majordiastereomer: ¹H NMR (300 MHz, CDCl₃) δ (ppm): 4.48 (s, 1H), 4.09 (dd,J=11.6, 3.1 Hz, 1H), 3.78-3.58 (m, 1H), 3.37 (dt, J=10.3, 6.5 Hz, 1H),3.06 (dtd, J=10.6, 7.6, 3.5 Hz, 1H), 2.98-2.68 (m, 2H), 2.11-1.72 (m,4H), 2.10-0.80 (br q, BH₃); ¹³C NMR (75 MHz, CDCl₃) δ (ppm): 66.9, 60.2,55.3, 27.4, 23.8; ¹¹B NMR (96 MHz, DMSO-d₆) δ (ppm): −16.43 (q, J=96.0Hz). HRMS (CI) calcd for C₅H₁₃BNO (M−H)⁺: m/z, 114.1085, found 114.1087.

2-Diethylaminoethanethiol-borane (2w) Colorless oil. ¹H NMR (400 MHz,CDCl₃) δ (ppm): 2.98-2.69 (m, 8H), 1.19 (t, J=7.3 Hz, 6H), 1.95-0.95 (brq, BH₃); ¹³C NMR (101 MHz, CDCl₃) δ (ppm): 61.9, 53.0, 18.7, 8.7; ¹¹BNMR (96 MHz, CDCl₃) δ (ppm): −13.45 (q, J=99.1, 93.3 Hz). HRMS (ESI)calcd for C₆H₁₇BNS (M−H)⁺: m/z, 146.1175, found 146.1176.

2,2-Dimethoxy-N,N-dimethylethylamine-borane (2x) Colorless liquid. ¹HNMR (300 MHz, CDCl₃) δ (ppm): 4.94-4.88 (m, 1H), 3.44-3.37 (m, 6H),2.90-2.83 (m, 2H), 2.64 (m, 6H), 2.20-1.10 (br q, BH₃); ¹³C NMR (75 MHz,CDCl₃) δ (ppm): 101.3, 65.2, 54.5, 53.0; ¹¹B NMR (96 MHz, CDCl₃) δ(ppm): −9.85 (q, J=99.0 Hz). HRMS (CI) calcd for C₆H₁₇BNO₂ (M−H)⁺: m/z,146.1347, found 146.1345.

Methyl 6-aminohexanoate-borane (2y) White solid. ¹H NMR (300 MHz, CDCl₃)δ (ppm): 3.87 (s, 2H), 3.68 (s, 3H), 2.81 (p, J=7.2 Hz, 2H), 2.34 (t,J=7.3 Hz, 2H), 1.75-1.56 (m, 4H), 1.44-1.31 (m, 2H), 2.10-0.80 (br q,BH₃); ¹³C NMR (101 MHz, CDCl₃) δ (ppm): 174.2, 51.8, 48.6, 33.8, 28.7,26.1, 24.4; ¹¹B NMR (96 MHz, CDCl₃) δ (ppm): −15.61 (q, J=98.0 Hz). HRMS(CI) calcd for C₇H₁₇BNO₂ (M−H)⁺: m/z, 158.1347, found 158.1349.

N-(3-Aminopropyl)benzamide-borane (2z) White solid. ¹H NMR (300 MHz,DMSO-d₆) δ (ppm): 8.53 (t, J=5.9 Hz, 1H), 7.89-7.76 (m, 2H), 7.58-7.38(m, 3H), 5.19 (s, 2H), 3.26 (q, J=6.5 Hz, 2H), 2.56-2.36 (m, 2H), 1.74(p, J=7.1 Hz, 2H), 1.75-0.80 (br q, BH₃); ¹³C NMR (101 MHz, DMSO-d₆) δ(ppm): 166.4, 134.4, 131.1, 128.3, 127.1, 45.4, 36.7, 28.3; ¹¹B NMR (96MHz, DMSO-d₆) δ (ppm): −19.26 (br, BH₃). HRMS (CI) calcd for C₁₀H₁₆BN₂O(M−H)⁺: m/z, 191.1350, found 191.1348.

3-(Dimethylamino)propanenitrile-borane (2aa) Colorless liquid. ¹H NMR(300 MHz, CDCl₃) δ (ppm): 3.11-2.88 (m, 4H), 2.66 (s, 6H), 2.19-0.94 (brq, BH₃); ¹³C NMR (75 MHz, CDCl₃) δ (ppm): 117.4, 59.5, 52.5, 14.2; ¹¹BNMR (96 MHz, CDCl₃) δ (ppm): −10.96 (q, J=98.6 Hz). HRMS (CI) calcd forC₅H₁₂BN₂ (M−H)⁺: m/z, 111.1088, found 111.1087.

2-(4-Nitrophenyl)ethylamine-borane (2ab) White solid. ¹H NMR (400 MHz,DMSO-d₆) δ (ppm): 8.10 (d, J=8.6 Hz, 2H), 7.45 (d, J=8.4 Hz, 2H), 5.32(s, 2H), 2.93 (dd, J=9.5, 6.4 Hz, 2H), 2.76-2.58 (m, 2H), 1.85-0.80 (brq, BH₃); ¹³C NMR (101 MHz, DMSO-d₆) δ 147.1, 146.2, 129.9, 123.6, 48.3,33.9; ¹¹B NMR (96 MHz, DMSO-d₆) δ (ppm): −19.58 (q, J=101.7, 95.1 Hz).HRMS (ESI) calcd for C₈H₁₂BN₂O₂ (M−H)⁺: m/z, 179.0992, found 179.0992.

(3-Aminopropyl)triethoxysilane-borane (2ac) Colorless liquid. ¹H NMR(400 MHz, CDCl₃) δ (ppm): 3.99-3.88 (m, 2H), 3.84 (qd, J=7.0, 2.9 Hz,6H), 2.82 (ddt, J=10.6, 6.9, 4.1 Hz, 2H), 1.76 (pd, J=7.1, 3.0 Hz, 2H),1.24 (td, J=7.0, 2.9 Hz, 9H), 0.66 (td, J=7.8, 3.0 Hz, 2H), 2.10-1.10(br q, BH₃); ¹³C NMR (101 MHz, CDCl₃) δ (ppm): 58.8, 50.9, 22.6, 18.4,7.7; ¹¹B NMR (96 MHz, CDCl₃) δ (ppm): −19.95 (q, J=100.5 Hz). HRMS (ESI)calcd for C₉H₂₆BNO₃SiNa (M+Na)⁺: m/z, 257.1709, found 257.1711.

3-(Pyridin-2-ylamino)propan-1-ol-borane (4) Colorless oil. ¹H NMR (300MHz, CDCl₃) δ (ppm): 8.09 (d, J=6.2 Hz, 1H), 7.57 (t, J=9.0 Hz, 1H),6.64 (d, J=8.8 Hz, 1H), 6.54 (t, J=6.6 Hz, 1H), 6.41 (s, 1H), 3.79 (t,J=5.9 Hz, 2H), 3.42 (q, J=6 Hz, 2H), 2.55 (s, 1H), 1.92 (p, J=6 Hz, 2H),2.80-1.50 (br q, BH₃); ¹³C NMR (75 MHz, CDCl₃) δ (ppm): 154.6, 145.9,139.8, 111.2, 107.2, 59.9, 39.9, 31.5; ¹¹B NMR (96 MHz, CDCl₃) δ (ppm):−17.92 (q, J=97.5, 91.7 Hz). HRMS (CI) calcd for C₈H₁₄BN₂O (M−H)⁺: m/z,165.1194, found 165.1189.

General procedure for hydride analysis of amine-boranes (Hydrolysisreaction):

An aqueous solution of amine-borane (2 mmol in 1 mL H₂O) was transferredto a round bottom flask with a septum inlet fitted with a connectingtube. The connecting tube was attached to an analytical gas burettefilled with CuSO4 solution. A solution of RuCl₃ (4.2 mg, 1 mol % in 2 mLH₂O) was syringed into the vial, all at once. The hydrogen generated wasmeasured using the analytical gas burette. The temperature of thereaction was maintained at 25° C.

Those skilled in the art will recognize that numerous modifications canbe made to the specific implementations described above. Theimplementations should not be limited to the particular limitationsdescribed. Other implementations may be possible.

What is claimed is:
 1. An amine-borane prepared according to the processof a. preparing about two equivalent of sodium borohydride and aboutfour equivalents of sodium bicarbonate; b. adding about one equivalentamine, wherein said amine carries a functional group selected from thegroup consisting of alkene, alkyne, nitro, hydroxyl, thiol, cyano(nitrile), acetal, ester, amide, and alkoxysilane; c. adding THF(tetrahydrofuran) with stirring to afford a reaction mixture of saidamine at about 0.5˜2 M (moles/liter); d. adding dropwise about 3˜4equivalents of water in a THF solution to the reaction mixture of step cunder vigorous stirring; and e. stirring for about 4 to 48 hours toafford an amine-borane, wherein said amine-borane may carry a functionalgroup selected from the group consisting of alkene, alkyne, nitro,hydroxyl, thiol, cyano (nitrile), acetal, ester, amide, andalkoxysilane.
 2. The amine-borane according to claim 1, wherein saidprocess is carried out at an ambient temperature.
 3. The amine-boraneaccording to claim 1, wherein said water-THF solution is about 14% (v/v)water in THF.
 4. The amine-borane according to claim 1, wherein saidamine may be a monoamine or a diamine.
 5. The amine-borane according toclaim 1, wherein said amine-borane is part of an aromatic molecule, analiphatic molecule, or a combination thereof.
 6. The amine-boraneaccording to claim 1, wherein said amine-borane is part of a cyclicstructure, a linear structure, a branched structure, or a combinationthereof.
 7. The amine-borane according to claim 1, wherein said water ina THF solution is about four equivalents of said amine when said aminecarries a functional group selected from the group consisting of alkene,alkyne, nitro, hydroxyl, thiol, cyano (nitrile), acetal, ester, amide,and alkoxysilane.
 8. The amine-borane according to claim 1, wherein saidamine carries one or more functional groups selected from the groupconsisting of alkene, alkyne, nitro, hydroxyl, thiol, cyano (nitrile),acetal, ester, amide, and alkoxysilane.
 9. The amine-borane according toclaim 1, wherein said amine-borane carries one or more functional groupsselected from the group consisting of alkene, alkyne, nitro, hydroxyl,thiol, cyano (nitrile), acetal, ester, amide, and alkoxysilane.